CHILDREN MYOPIA CONTROL
Primary Purpose
Myopia
Status
Active
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Lenses
Sponsored by
About this trial
This is an interventional treatment trial for Myopia focused on measuring MYOPIA CONTROL
Eligibility Criteria
Inclusion Criteria:
- Informed consent form signed and fully comprehended by the parent/legal representative of the participant
- Age from 6 to 12 years old
- Both male and female
- Spherical Equivalent refractive error (cycloplegic objective) of -0.50D to -5.00D
- Astigmatism not higher than -1.50D
- Corrected Visual Acuity of not less than 6/7.5 or 20/25
- Willing to wear the trial spectacles for the defined period according the protocol plan
Exclusion Criteria:
- Current participation in another clinical trial
- Any general health or ocular health pathology that could affect the treatment
- Allergy or intolerance to cycloplegic eye drops (name should be stated here)
- Strabismus
- Amblyopia
- History of ocular injury or ocular surgery
- Previously been treated with any myopia control treatments (Orthokeratology, myopia control spectacle/contact lenses, multifocal lenses, bifocal lenses, atropine)
Sites / Locations
- "Maor" Institute Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Myopia control design spectacle lens
Single Vision design spectacle lens
Arm Description
Test lenses
Control lenses
Outcomes
Primary Outcome Measures
Refractive error
Objective cycloplegic refractive error (Sphere equivalent)
Secondary Outcome Measures
Axial length
Full Information
NCT ID
NCT05477329
First Posted
July 26, 2022
Last Updated
July 28, 2022
Sponsor
Shamir Optical Industry Ltd
1. Study Identification
Unique Protocol Identification Number
NCT05477329
Brief Title
CHILDREN MYOPIA CONTROL
Official Title
EVALUATING THE EFFECT OF A MYOPIA CONTROL SPECTACLE LENS COMPARED TO A SINGLE VISION SPECTACLE LENS AMONG CHILDREN IN ISRAEL
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 20, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shamir Optical Industry Ltd
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The purpose of this trial is evaluating the clinical effect of a myopia control spectacle lens compared to a single vision spectacle lens in slowing down the progression of myopia in children living in Israel.
Detailed Description
TRIAL PLAN
Screening visit (VISIT 1)
Enrollment criteria verification
Signing informed consent
Baseline documentation of medical history, parental and siblings myopia, indoor and outdoor activities profile and socioeconomic profile
Lensmeter measurements of participants spectacles
Performing baseline measurements including best corrected VA, objective & subjective refraction under cycloplegia, PR under cycloplegia*, slit lamp examination, functional tests: cover test, titmus test, worth four dot test, axial length** and pupil size measurements
Frame selection and frame measurements
Lens order completion and sending to manufacturing
Randomization Procedures (following VISIT 1) Randomization procedures should be performed by the trial coordinator following visit 1. The participant will then be allocated to the test or control group.
Manufacturing Procedures (following VISIT 1) The manufacturing technician will take care of the manufacturing processes according to the lens type (test or control) and the mounting on the frame. The test spectacles will then be sent to the site for delivery.
Delivery visit (VISIT 2) performed ~10 days after screening visit
Trial spectacles delivery
Subjective questionnaire while wearing the trial spectacles
Best corrected far and near VA (with the trial spectacles)
Confrontation visual field test with the trial spectacles
Giving instructions about wearing the trial spectacles
Documenting adverse events if relevant
Follow-up visit performed 6 months (±1 week) after the previous visit (VISITS 3,4,5,6)
Documentation of any change medical history since last visit
Subjective questionnaire regarding the wearing period with the trial spectacles (feedback performing follow-up measurements including best corrected far and near VA, objective & subjective refraction under cycloplegia, PR under cycloplegia*, slit lamp examination, functional tests: cover test, titmus test, worth four dot test, axial length and pupil size measurements
If the subjective refraction will find a SE (Sphere Equivalent) change from last refraction of at least -0.50D, a new lens order should be made for new lenses, and a delivery visit should be set in order to deliver the new test spectacles. The procedures mentioned above in the delivery visit (visit 2) should then be performed.
Documenting adverse events if relevant
Additional unscheduled visits
May be scheduled as needed if special needs occur
Procedures will be defined by the investigator
Documenting adverse events if relevant
Total duration of trial per patient: 24 months.
ETHICAL ISSUES
This trial will be conducted according to the applicable local regulations and the GCP. All essential documents will be reviewed and approved by the ethics committee prior to the beginning of the trial. Any amendments of these documents will be reviewed and approved by the ethics committee prior to implantation in the trial.
Informed Consent The investigator will give the participant and their parent/legal guardian a full explanation about the trial and will answer all their question regarding participating in the trial.
The investigator will explain that the participant will be able to withdraw from the trial at any stage for any reason.
The participants parent/legal guardian will sign the informed consent form and will receive a signed copy of it.
Data confidentiality All identification details about the participants in the trial will be held by the investigator in a secured log file kept at the trial site.
Access to the identification details will not be allowed to any unauthorized party and will not be disclosed in any report/document relating to the trial.
Terminating the participation in the trial
These are the cases in which an early termination of the participation in the trial may occur:
Should the myopia progression of the participant will be more than 1.00 D after 1 year or other significant refractive changes (such as more than 0.5[D] cylinder) - the investigator will recommend the participant to discontinue the participation in the trial and to consider using other myopia control treatments such as low dose Atropine drops.
Should the far/near VA with the trial spectacles will be less than the best corrected VA of the participant, the investigator will consider recommending the participant to discontinue the participation in the trial.
RISK EVALUATION/ ADVERSE EVENTS
The optical design of the test lens, with the gradual positive peripheral power, induce a certain amount of aberrations in the peripheral areas of the lens. These aberrations were designed such that a good level of compliance will be achieved so that the participant will be able to wear the lens.
Adverse events are unlikely to occur, yet it should be mentioned that a participant should not wear this lens in case of one/more of the following exist:
Feeling significant amount of discomfort while wearing the lens such that the safety of the participant might be at risk.
Vestibular disorders The participants in the trial will be free to contact the investigator at any time during the wearing period in order to report any unexpected events that might occur. The investigator will decide based on the report whether the child should be excluded from continuing the trial.
Furthermore, it should be noted that a parallel clinical trial is being conducted these days in AIER hospital in China, managed and supervised by Brien Holden Vision Institution (Australia). The trial is similar to our trial, with the same trial product, on a group of 140 participants with the same enrollment criteria, including similar trial procedures and trial plan. The trial started at November 2020, and as for now most of the participants has worn the test spectacles for a few months with no adverse events reported.
DATA MANAGEMENT
Database An electronic data base will be held and maintained, into which all the source data will be electronically transferred from the measuring devices, or if not possible, will be typed in and source data (printouts or location of data) will be kept in the participants file. At any case, all source data (printouts or location of data) should be kept in the participants file.
The electronic data base will be backed up on a daily basis
Access to data:
The investigator will be able to allow access to data to the Sponsor (without identification data) as per request.
The investigator will be able to allow access to data to the Monitoring staff according to the monitoring plan that will be defined.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
MYOPIA CONTROL
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This will be a controlled, randomized, double-masked trial. The Test group will wear the myopia control spectacle lens and the Control group will wear the single vision spectacle lens.
Masking
ParticipantCare ProviderInvestigator
Masking Description
This will be a controlled, randomized, double-masked trial. The Test group will wear the myopia control spectacle lens and the Control group will wear the single vision spectacle lens.
Allocation
Randomized
Enrollment
136 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Myopia control design spectacle lens
Arm Type
Experimental
Arm Description
Test lenses
Arm Title
Single Vision design spectacle lens
Arm Type
Other
Arm Description
Control lenses
Intervention Type
Device
Intervention Name(s)
Lenses
Intervention Description
The test lens is manufactured in a standard FreeForm technology (exactly like a standard progressive addition lens which is similar in terms of the graduall power profile induced in both lens). It does not demand any special manufacturing processes.
Primary Outcome Measure Information:
Title
Refractive error
Description
Objective cycloplegic refractive error (Sphere equivalent)
Time Frame
3 seconds
Secondary Outcome Measure Information:
Title
Axial length
Time Frame
3 seconds
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Informed consent form signed and fully comprehended by the parent/legal representative of the participant
Age from 6 to 12 years old
Both male and female
Spherical Equivalent refractive error (cycloplegic objective) of -0.50D to -5.00D
Astigmatism not higher than -1.50D
Corrected Visual Acuity of not less than 6/7.5 or 20/25
Willing to wear the trial spectacles for the defined period according the protocol plan
Exclusion Criteria:
Current participation in another clinical trial
Any general health or ocular health pathology that could affect the treatment
Allergy or intolerance to cycloplegic eye drops (name should be stated here)
Strabismus
Amblyopia
History of ocular injury or ocular surgery
Previously been treated with any myopia control treatments (Orthokeratology, myopia control spectacle/contact lenses, multifocal lenses, bifocal lenses, atropine)
Facility Information:
Facility Name
"Maor" Institute Clinic
City
Rishon LeZion
Country
Israel
12. IPD Sharing Statement
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CHILDREN MYOPIA CONTROL
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